NP-MRD: Showing NP-Card for 8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate (NP0220219)

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Record Information

Version

2.0

Created at

2022-09-05 21:28:12 UTC

Updated at

2022-09-05 21:28:12 UTC

NP-MRD ID

NP0220219

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate

Description

[8'-(Acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-octahydrodispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-yl]methyl acetate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate is found in Teucrium massiliense. Based on a literature review very few articles have been published on [8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-octahydrodispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-yl]methyl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052223282D          

 33 37  0  0  0  0            999 V2000
    0.5549    1.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3789    1.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8259    2.2001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7559    0.7729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5799    0.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9569   -0.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9110    0.8224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1746    1.1945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1287    2.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7516    2.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8190    2.4699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014    1.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3377    0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0281    1.3537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3837    0.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1175    0.4554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7028   -0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5172    0.0058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1026   -0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8364   -0.1986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7045    0.6158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8893    0.7421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3308   -0.8624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5155   -0.7361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1434   -1.4724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6933   -0.3733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7393   -1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0489   -1.6487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0949   -2.4724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3125   -1.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2666   -0.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4429   -0.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149    0.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 22  2  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
 15 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  0  0  0  0
M  END


  Mrv1652309052223282D          

 33 37  0  0  0  0            999 V2000
    0.5549    1.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3789    1.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8259    2.2001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7559    0.7729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5799    0.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9569   -0.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9110    0.8224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1746    1.1945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1287    2.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7516    2.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8190    2.4699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014    1.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3377    0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0281    1.3537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3837    0.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1175    0.4554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7028   -0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5172    0.0058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1026   -0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8364   -0.1986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7045    0.6158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8893    0.7421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3308   -0.8624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5155   -0.7361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1434   -1.4724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6933   -0.3733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7393   -1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0489   -1.6487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0949   -2.4724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3125   -1.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2666   -0.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4429   -0.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149    0.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 22  2  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
 15 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220219

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(OC(C)=O)C2(COC(C)=O)C(CC(O)CC22CO2)C11CC(OC1=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O9/c1-13-6-20(32-15(3)26)24(12-30-14(2)25)19(7-17(27)8-22(24)11-31-22)23(13)9-18(33-21(23)28)16-4-5-29-10-16/h4-5,10,13,17-20,27H,6-9,11-12H2,1-3H3

> <INCHI_KEY>
HUPBOJIWABTVPP-UHFFFAOYSA-N

> <FORMULA>
C24H30O9

> <MOLECULAR_WEIGHT>
462.495

> <EXACT_MASS>
462.188982546

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.47506322425481

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-octahydrodispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-yl]methyl acetate

> <JCHEM_LOGP>
0.7052487933333328

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.150381729024868

> <JCHEM_PKA_STRONGEST_BASIC>
-2.733023031724522

> <JCHEM_POLAR_SURFACE_AREA>
124.80000000000001

> <JCHEM_REFRACTIVITY>
111.10769999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'H-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-ylmethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       1.036   2.888   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.574   2.813   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.408   4.107   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.278   1.443   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.816   1.367   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.520  -0.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.434   1.535   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.059   2.230   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.974   3.767   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.270   5.137   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.262   4.610   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.723   2.378   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.097   1.684   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.386   2.527   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.183   0.146   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.553   0.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.645  -0.235   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.165   0.011   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.258  -1.074   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.628  -0.371   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      14.382   1.150   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      12.860   1.385   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.951  -1.610   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.429  -1.374   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.734  -2.749   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.894  -0.697   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.980  -2.235   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.691  -3.078   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.777  -4.615   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.317  -2.383   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.231  -0.846   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.693  -0.931   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.388   0.443   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26   31                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   24   26                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   18                                                       
CONECT   23   17   24                                                       
CONECT   24   23   15   25                                                  
CONECT   25   24                                                            
CONECT   26   15    6   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30    6   32   33                                             
CONECT   32   31   33                                                       
CONECT   33   32   31                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Value	Source
[8'-(Acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-octahydrodispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-yl]methyl acetic acid	Generator

Chemical Formula

C₂₄H₃₀O₉

Average Mass

462.4950 Da

Monoisotopic Mass

462.18898 Da

IUPAC Name

[8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-octahydrodispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-yl]methyl acetate

Traditional Name

8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'H-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolane]-8'a-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

CC1CC(OC(C)=O)C2(COC(C)=O)C(CC(O)CC22CO2)C11CC(OC1=O)C1=COC=C1

InChI Identifier

InChI=1S/C24H30O9/c1-13-6-20(32-15(3)26)24(12-30-14(2)25)19(7-17(27)8-22(24)11-31-22)23(13)9-18(33-21(23)28)16-4-5-29-10-16/h4-5,10,13,17-20,27H,6-9,11-12H2,1-3H3

InChI Key

HUPBOJIWABTVPP-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Teucrium massiliense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Furan
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.71	ChemAxon
pKa (Strongest Acidic)	15.15	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	124.8 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	111.11 m³·mol⁻¹	ChemAxon
Polarizability	46.48 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

85209523

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate (NP0220219)

MOL for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

3D MOL for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

3D SDF for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

3D-SDF for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

PDB for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

3D PDB for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

SMILES for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

INCHI for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

Structure for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)

3D Structure for NP0220219 (8'-(acetyloxy)-5''-(furan-3-yl)-3'-hydroxy-6'-methyl-2''-oxo-hexahydro-2'h-dispiro[oxirane-2,1'-naphthalene-5',3''-oxolan]-8'a-ylmethyl acetate)